Busch Lab

ZMP

GPRIN2

Ensembl ID:
ENSDARG00000086973
Description:
G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:23730]
Human Orthologues:
GPRIN1, GPRIN2
Human Descriptions:
G protein regulated inducer of neurite outgrowth 1 [Source:HGNC Symbol;Acc:24835]
G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:23730]
Mouse Orthologues:
Gprin1, Gprin2
Mouse Descriptions:
G protein regulated inducer of neurite outgrowth 2 Gene [Source:MGI Symbol;Acc:MGI:2444560]
G protein-regulated inducer of neurite outgrowth 1 Gene [Source:MGI Symbol;Acc:MGI:1349455]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18582 Nonsense Available for shipment Available now
sa42312 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18582
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000121508 Nonsense 92 550 1 1
Genomic Location (Zv9):
Chromosome 13 (position 53360372)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 45679180
GRCz11 14 50830412
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGRTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGAT[C/T]AGGAGATCACCAWTCTRGTGACCAATCMTGAYTGCAATTTAGAGGAGGAA
Long Flanking Sequence:
GTGTTTTATAATAGTGTTTGTTTTTACAATGAATAAAATTGAACCCAGAATAAATCTCTGATGTAATACGCCTCCTAAAATGTCAGTCACTTTGGACAAAAATATCAGCTAAATCTGTTATATGTTTTCAATAAGTACTAATGCATTTATGTGCATGCTTTCCAGCTAACCCTCAGTGGTGTGAAACACATTTCACTTTGCTTCGCCACAAACTCATCTCTGAACTCATGGAGGGTCCGGTTTTGACAGAGAGTGAAGTTTGGAAAGTTGGCTCGGAGACCAGCACAAGTATAAACCCAGAAGACCGAAGCATTGACTATCCTCTCATTAATGACACTGATGAAAAAGTGAAAGCACCAGAGAGTGCAGTCCAAGAGGAGATCATCCAACAGTCTGTGAATCCACCTGAACTGCGAATCGAGGATTTATCTTCCCCTCAAACTGAAATGGAGGTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGAT[C/T]AGGAGATCACCATTCTGGTGACCAATCATGATTGCAATTTAGAGGAGGAAGAGGATGAGGACACAAATGAAGAGCAGACGGCTTGTACTGAAGCTGTAATATCTAGTGTTGATGTTCGAGAACTGATTGATGAGGATAATCTTGATGGATCAATTGTTGTGGCCAACATGATTGAAGTAAGTCAAATCCAGAAAACCAACGTCGTAAACAACACCTCAACTAATACAACAACTGAAGAACAACCTAAATCTCAAGAGGATCCAGACCCAATTTGCACAAAGTCAAACCCACCACAGGAATCGGATGTTTGTAGCACACAAAGTCTGAAAGATCAGCCCACACAGTCTGAGGATGTAGGAAAAGTCGATGCAAATAAAAGCGAACCGGCTAAAGAGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACACAAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACTCCACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42312
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000121508 Nonsense 240 550 1 1
Genomic Location (Zv9):
Chromosome 13 (position 53360816)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 45679624
GRCz11 14 50830856
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACA[C/T]AAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACT
Long Flanking Sequence:
AAATGGAGGTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGATCAGGAGATCACCATTCTGGTGACCAATCATGATTGCAATTTAGAGGAGGAAGAGGATGAGGACACAAATGAAGAGCAGACGGCTTGTACTGAAGCTGTAATATCTAGTGTTGATGTTCGAGAACTGATTGATGAGGATAATCTTGATGGATCAATTGTTGTGGCCAACATGATTGAAGTAAGTCAAATCCAGAAAACCAACGTCGTAAACAACACCTCAACTAATACAACAACTGAAGAACAACCTAAATCTCAAGAGGATCCAGACCCAATTTGCACAAAGTCAAACCCACCACAGGAATCGGATGTTTGTAGCACACAAAGTCTGAAAGATCAGCCCACACAGTCTGAGGATGTAGGAAAAGTCGATGCAAATAAAAGCGAACCGGCTAAAGAGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACA[C/T]AAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACTCCACCAGAAGCTTCTGGAACTTTCATTTTTCCAAGCACTTTTGGAAAGCTCGCTAATAAATGCAACCAGGAGGACTTAGAGACTAAAAATGTGGAGATGCATTCGGTGGCCACAGCTCCAATGACTCCTTTAGTTCTGAACGCTCCAGAGACGCATTCTGTAGCCACTGCTCCAATGACTCCTTTAGTACTGAATGCTCCAGAGCTGCATTCGATAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCTCCAGAGATGCATTCGACAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCTCCAGAGATGCATTCGACAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCCCCAGAGATGCATTCGATAGGCACAGCTCCAATGACTCCTATAGTTCTGAATGCCCCAGAGATGTGTTCTGTAGCCACAGCTCCAATGACT
Associated Phenotype:
Not determined